Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2.

Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2. Am J Med Genet A. 2008 Jul 01; 146A(13):1637-54.

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subject areas

Abnormalities, Multiple
Adolescent
Adult
Aneuploidy
Brain
Child
Child, Preschool
Chromosome Aberrations
Chromosome Breakage
Chromosome Deletion
Chromosomes, Artificial, Bacterial
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 21
Chromosomes, Human, Pair 4
Chromosomes, Human, Pair 6
Female
Humans
In Situ Hybridization, Fluorescence
Infant
Infant, Newborn
Karyotyping
Male
Malformations of Cortical Development
Phenotype
Translocation, Genetic

authors with profiles

William B. Dobyns